Evidence map›Paper›PMID 34748864›Full record

ArticleProgress in neuro-psychopharmacology & biological psychiatry2022

Striatal glutamate, subcortical structure and clinical response to first-line treatment in first-episode psychosis patients.

Francisco Reyes-Madrigal, Elisa Guma, Pablo León-Ortiz, Gladys Gómez-Cruz, Ricardo Mora-Durán, Ariel Graff-Guerrero, Lawrence S Kegeles, M Mallar Chakravarty, Camilo de la Fuente-Sandoval

Open access · greenAbstract read
In one paragraph

Article in Progress in neuro-psychopharmacology & biological psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 3 pooled it
1.8field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 3 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Review
  6. Review
  7. Glutamatergic basis of antipsychotic response in first-episode psychosis: a dual voxel study of the anterior cingulate cortex.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  8. Article
  9. Illness Phase as a Key Assessment and Intervention Window for Psychosis.Biological psychiatry global open science · 2023
    Review
  10. Anterior cingulate glutamate metabolites as a predictor of antipsychotic response in first episode psychosis: data from the STRATA collaboration.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  11. Glutamatergic dysfunction in Schizophrenia.Translational psychiatry · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 3 countries.

Francisco Reyes-MadrigalLaboratory of Experimental Psychiatry, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico.
Elisa GumaIntegrated Program in Neuroscience, McGill University, Montreal, QC, Canada; Computational Brain Anatomy (CoBrA) Lab, Cerebral Imaging Centre, Douglas Research Centre, Montreal, QC, Canada.
Pablo León-OrtizLaboratory of Experimental Psychiatry, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico.
Gladys Gómez-CruzLaboratory of Experimental Psychiatry, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico.
Ricardo Mora-DuránEmergency Department, Hospital Fray Bernardino Álvarez, Mexico City, Mexico.
Ariel Graff-GuerreroMultimodal Neuroimaging Schizophrenia Group, Centre for Addiction and Mental Health, Toronto, ON, Canada.
Lawrence S KegelesDepartment of Psychiatry, Columbia University College of Physicians and Surgeons, New York, USA.
M Mallar ChakravartyIntegrated Program in Neuroscience, McGill University, Montreal, QC, Canada; Computational Brain Anatomy (CoBrA) Lab, Cerebral Imaging Centre, Douglas Research Centre, Montreal, QC, Canada; Department of Psychiatry, McGill University, Montreal, QC, Canada; Department of Biological and Biomedical Engineering, McGill University, Montreal, QC, Canada.
Camilo de la Fuente-SandovalLaboratory of Experimental Psychiatry, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico; Neuropsychiatry Department, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico. Electronic address: fcamilo@unam.mx.
Instituto Nacional de Neurología y Neurocirugía · MXMcGill University · CACentre for Addiction and Mental Health · CAColumbia University · USUniversidad Fray Luca Paccioli · MX

Funding

Biomarkers of Conversion Risk and Treatment Response in Early-Stage SchizophreniaR01MH110270 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI GIRGIS, RAGY RAMSIS, KEGELES, LAWRENCE S · 2017 to 2021
$3.7M
Mechanisms of copper dysregulation in schizophreniaR21MH117434 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ROBERTS, ROSALINDA C · 2018 to 2019
$400k
Inflammatory Biomarkers in First Episode Psychosis: A Mexico/US CollaborationR21MH102374 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CADENHEAD, KRISTIN S., DE LA FUENTE, CAMILO · 2014 to 2015
$253k
NIMH NIH HHS R01 MH110270NIMH NIH HHS R21 MH102374NIMH NIH HHS R21 MH117434
6 · The paper itself

Abstract

introductionRecent studies have observed that patients with treatment-resistant schizophrenia as well as patients with schizophrenia who do not respond within a medication trial exhibit excess activity of the glutamate system. In this study we sought to replicate the within-trial glutamate abnormality and to investigate the potential for structural differences and treatment-induced changes to improve identification of medication responders and non-responders.

methodsWe enrolled 48 medication-naïve patients in a 4-week trial of risperidone and classified them retrospectively into responders and non-responders using clinical criteria. Proton magnetic resonance spectroscopy and T

resultsPatients were classified as 29 responders and 19 non-responders. Striatal glutamate was higher in the non-responders than responders both pre- and post-treatment (F

conclusionsCombining anatomic measures with glutamate levels offers the potential to enhance classification of responders and non-responders to antipsychotic medications as well as to provide mechanistic understanding of the interplay between neuroanatomical and neurochemical changes induced by these medications. Ethical statement The study was approved by the Ethics and Scientific committees of the Instituto Nacional de Neurología y Neurocirugía in Mexico City. All participants over 18 years fully understood and signed the informed consent; in case the patient was under 18 years, informed consent was obtained from both parents. Participants did not receive a stipend.

Indexed as

Corpus StriatumPsychotic DisordersSchizophrenia, Treatment-ResistantAdultBrainFemaleGlutamic AcidHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMaleProton Magnetic Resonance SpectroscopyRetrospective StudiesRisperidoneSerotonin AntagonistsSurveys and QuestionnairesGlutamic AcidRisperidoneSerotonin AntagonistsAntipsychotic treatmentBrain volume analysisFirst episodeGlutamateMagnetic resonance spectroscopySchizophrenia

Identifiers

PMID34748864
PMCPMC8643337
OpenAlexW3214706576

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.